MedTech Regulatory Affairs Specialist – On-Site, Bonus

Newton Colmore Consulting is seeking a Regulatory Affairs Specialist for a MedTech client in Cambridgeshire. You will ensure compliance with UK/European standards, drive regulatory strategy, and support audits across multiple product ranges.

Ideal candidates have 2–5 years of experience in regulatory affairs or QA for medical devices, with a background in engineering or biomedical fields. The role is based in the office and offers a strong benefits package.

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